Avanza for sponsors

We help the pharmaceutical and biotech community create moments of discovery that advance the field of medicine.

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Every mission begins with a vision. Ours is to help you achieve yours.

We work with medical research sponsors and CROs to provide them access to seasoned and esteemed professionals with relevant scientific, therapeutics and operational expertise and training throughout the entire study lifecycle.

Pillars of service

Our commitment goes beyond mission statements. We serve research sponsors and CROs in a variety of methods. These are our pillars of service, and they act as our compass for delivering performance excellence.

  • Capabilities
    Our clinical research staff has access to a unique set of equipment and broad range services inside and outside the clinic setting.
  • Compatibility
    Our team is easy to work with and responds to our clients’ needs in a timely manner.
  • Expertise
    Avanza works with highly experienced investigators with deep therapeutic knowledge to provide research support (in varying capacities) to a variety of disciplines in both outpatient and inpatient settings.
  • Quality
    We pride ourselves on the quality of the data collected by our trained project management team.
  • Reliability
    Our goal is to consistently deliver excellence through meticulous and quality data, and strict adherence to the scientific process and research protocol.

Benefits

Access to Qualified Patients

Using our database of over 4,000 patients, we hand select and match research studies with the appropriate patient populations to ensure the integrity of the research process.

Research Focused

We are researchers first. Our team is 100% focused on conducting and managing clinical trials to ensure the integrity of each and every study.

Process-Led Design

We take process seriously, working with our sponsors and clients through a multi-phased approach to ensure the strictest compliance to each study and research protocol.

Complete Lifecycle

Our research team follows every study through every phase of its timeline: opportunity identification, feasibility assessment, study start-up, study execution and study-closeout.

Interested in engaging us in research? Contact us.

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Quick Facts

Standard Staff & Investigator Training and Compliance Requirements:
  • ICH-GCP
  • FDA
  • IRB
  • OSHA
  • HIPAA
Site Equipment:
  • Centrifuges
  • Electrocardiographs
  • Vital Sign Monitors
  • Refrigerators
  • Freezers -20˚C
  • Bone Densitometer
  • Pulmonary Function Testing
  • Exercise Stress Testing
  • Spirometers
  • Scales
  • Stadiometers
  • Infant Scale
  • Transilluminator
Therapeutic Areas:
  • Bariatric Medicine
  • Cardiology
  • Critical Care
  • Emergency Medicine
  • Endocrinology
  • General Surgery
  • Geriatrics
  • Infectious Disease
  • Internal Medicine
  • Interventional Radiology
  • Nephrology
  • Neurophysiology
  • Orthopedics
  • Pain Management
  • Pediatrics
  • Pulmonary
  • Radiology
  • Urology
  • Vascular Surgery

Partner with us

Participate
Interested in engaging us in research? Let's talk.
Contact Us